Study Start Up CRA
ICON
Clinical Research Associate at a large contract research organization supporting sponsor-dedicated clinical trial operations. The role involves study setup, monitoring, site coordination, and ensuring regulatory compliance across assigned programs.
Responsibilities
- Coordinate study setup and monitoring activities independently while maintaining documentation
- Complete study status reports and manage sponsor-generated queries efficiently
- Develop and maintain relationships with investigators, site staff, and key stakeholders
- Review study documentation and assess feasibility for new proposals
- Ensure compliance with protocols, procedures, and regulatory requirements
Requirements
- University degree in medicine, science, or equivalent field
- Knowledge of ICH-GCP guidelines and ability to review medical data
- Fluent written and verbal English communication
- Strong interpersonal and problem-solving skills
- Willingness to travel approximately 60% of the time
- Clinical trial monitoring experience
Vacancy posted 4 hours ago
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